Canonical Allele Identifier: CA2579071978
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675990del , CM000669.2:g.152675990del GRCh38
NC_000007.13:g.152373075del , CM000669.1:g.152373075del GRCh37
NC_000007.12:g.152004008del NCBI36
NG_027988.1:g.5178del
NG_027988.2:g.5178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+53del ENSP00000513758.1:n.-48+53del
ENST00000698507.1:n.107+53del
ENST00000359321.2:c.39+53del MANE Select ENSP00000352271.1:n.39+53del
ENST00000359321.1:c.39+53del ENSP00000352271.1:n.39+53del
NM_005431.1:c.39+53del NP_005422.1:n.39+53del
NM_005431.2:c.39+53del MANE Select NP_005422.1:n.39+53del